Variant report

Variant	nsv960763
Chromosome Location	chr19:40168890-40177573
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:305)
Chromatin interactive
region (count:6)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr19:40177332-40177734	GM12878	blood:	n/a	n/a
2	ATF2	chr19:40169169-40171721	GM12878	blood:	n/a	n/a
3	ATF2	chr19:40169348-40171215	GM12878	blood:	n/a	n/a
4	BATF	chr19:40169465-40170751	GM12878	blood:	n/a	n/a
5	BCL11A	chr19:40169661-40170751	GM12878	blood:	n/a	n/a
6	BCL3	chr19:40177478-40177702	GM12878	blood:	n/a	chr19:40177575-40177584
7	BCL3	chr19:40170081-40170842	GM12878	blood:	n/a	n/a
8	BCL3	chr19:40169586-40170952	GM12878	blood:	n/a	chr19:40169623-40169631
9	BCLAF1	chr19:40169381-40171764	GM12878	blood:	n/a	chr19:40169623-40169631
10	BCLAF1	chr19:40169441-40171302	GM12878	blood:	n/a	chr19:40169623-40169631
11	BHLHE40	chr19:40171344-40171662	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:40169675-40171090	GM12878	blood:	n/a	n/a
13	BRCA1	chr19:40172330-40172407	GM12878	blood:	n/a	n/a
14	BRCA1	chr19:40169819-40170833	GM12878	blood:	n/a	n/a
15	BRCA1	chr19:40169254-40169347	GM12878	blood:	n/a	n/a
16	CEBPB	chr19:40174793-40175365	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr19:40169429-40170617	GM12878	blood:	n/a	n/a
18	CHD1	chr19:40169671-40171710	GM12878	blood:	n/a	n/a
19	CHD2	chr19:40169141-40171016	GM12878	blood:	n/a	n/a
20	CHD2	chr19:40172217-40172294	GM12878	blood:	n/a	n/a
21	CHD2	chr19:40171410-40171603	GM12878	blood:	n/a	n/a
22	CTCF	chr19:40169301-40169429	GM12878	blood:	n/a	n/a
23	CTCF	chr19:40169260-40169410	GM12865	blood:	n/a	n/a
24	CTCF	chr19:40169297-40169430	GM19238	blood:	n/a	n/a
25	CTCF	chr19:40169220-40169370	HepG2	liver:	n/a	n/a
26	CTCF	chr19:40169278-40169430	GM12891	blood:	n/a	n/a
27	CTCF	chr19:40169240-40169390	GM12873	blood:	n/a	n/a
28	CTCF	chr19:40168940-40169090	GM12875	blood:	n/a	n/a
29	CTCF	chr19:40169262-40169449	GM12892	blood:	n/a	n/a
30	CTCF	chr19:40169240-40169390	HEK293	kidney:	n/a	n/a
31	CTCF	chr19:40170525-40170592	GM19239	blood:	n/a	n/a
32	CTCF	chr19:40169320-40169470	HepG2	liver:	n/a	n/a
33	CTCF	chr19:40169210-40169547	GM12878	blood:	n/a	n/a
34	CTCF	chr19:40169320-40169470	A549	lung:	n/a	n/a
35	CTCF	chr19:40169298-40169448	HepG2	liver:	n/a	n/a
36	CTCF	chr19:40170639-40170698	GM12892	blood:	n/a	n/a
37	CTCF	chr19:40169220-40169370	GM12873	blood:	n/a	n/a
38	CTCF	chr19:40169276-40169455	HepG2	liver:	n/a	n/a
39	CTCF	chr19:40169283-40169415	GM19240	blood:	n/a	n/a
40	CTCF	chr19:40169320-40169470	GM12873	blood:	n/a	n/a
41	CTCF	chr19:40170508-40170520	GM19239	blood:	n/a	n/a
42	CUX1	chr19:40169025-40171357	GM12878	blood:	n/a	chr19:40171034-40171043
43	EBF1	chr19:40168815-40171812	GM12878	blood:	n/a	n/a
44	EBF1	chr19:40169530-40170859	GM12878	blood:	n/a	n/a
45	EBF1	chr19:40169633-40170363	GM12878	blood:	n/a	n/a
46	EGR1	chr19:40170089-40170471	GM12878	blood:	n/a	n/a
47	ELK1	chr19:40170445-40170698	GM12878	blood:	n/a	n/a
48	ELK1	chr19:40169937-40170198	GM12878	blood:	n/a	n/a
49	ELK1	chr19:40171582-40171609	GM12878	blood:	n/a	n/a
50	EP300	chr19:40174929-40175340	Hela-S3	cervix:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40169839-40169889	CMK	blood:	n/a
2	chr19:40169418-40169468	A549	lung:	n/a
3	chr19:40174352-40174402	PANC-1	pancreas:	n/a
4	chr19:40169839-40169889	HEK293	kidney:	embryo
5	chr19:40169839-40169889	GM12878	blood:	n/a
6	chr19:40174352-40174402	Jurkat	blood:	n/a
7	chr19:40169912-40169962	SAEC	small airway:	n/a
8	chr19:40174352-40174402	NT2-D1	testis:	n/a
9	chr19:40169912-40169962	SK-N-SH	brain:	n/a
10	chr19:40169912-40169962	AG10803	skin:	n/a
11	chr19:40169912-40169962	HCPEpiC	choroid plexus:	n/a
12	chr19:40169418-40169468	AoSMC	blood vessel:	n/a
13	chr19:40168876-40168926	HepG2	liver:	n/a
14	chr19:40169418-40169468	ProgFib	skin:	n/a
15	chr19:40169418-40169468	HCM	heart:	n/a
16	chr19:40169418-40169468	SK-N-MC	brain:	n/a
17	chr19:40169912-40169962	Hela-S3	cervix:	n/a
18	chr19:40168876-40168926	NT2-D1	testis:	n/a
19	chr19:40169418-40169468	RPTEC	kidney:	n/a
20	chr19:40168876-40168926	HRPEpiC	eye:	n/a
21	chr19:40174352-40174402	HEK293	kidney:	embryo
22	chr19:40169912-40169962	GM06990	blood:	n/a
23	chr19:40169839-40169889	GM12892	blood:	n/a
24	chr19:40174352-40174402	AG04449	skin:	fetal
25	chr19:40168876-40168926	MCF-7	breast:	n/a
26	chr19:40174352-40174402	GM12891	blood:	n/a
27	chr19:40169912-40169962	ovcar-3	ovarian:	n/a
28	chr19:40169912-40169962	HL-60	blood:	n/a
29	chr19:40169839-40169889	HUVEC	blood vessel:	n/a
30	chr19:40169839-40169889	PrEC	prostate:	n/a
31	chr19:40169839-40169889	NHDF-neo	bronchial:	n/a
32	chr19:40169418-40169468	SK-N-SH_RA	brain:	n/a
33	chr19:40169912-40169962	MCF10A-Er-Src	breast:	n/a
34	chr19:40168876-40168926	GM19239	blood:	n/a
35	chr19:40168876-40168926	AG09309	skin:	n/a
36	chr19:40169418-40169468	SKMC	muscle:	n/a
37	chr19:40169839-40169889	NB4	blood:	n/a
38	chr19:40169418-40169468	SK-N-SH	brain:	n/a
39	chr19:40174352-40174402	AG09319	gingival:	n/a
40	chr19:40174352-40174402	HepG2	liver:	n/a
41	chr19:40174352-40174402	PFSK-1	brain:	n/a
42	chr19:40169912-40169962	HRCEpiC	kidney:	n/a
43	chr19:40169839-40169889	NHBE	bronchial:	n/a
44	chr19:40169418-40169468	NHDF-neo	bronchial:	n/a
45	chr19:40169418-40169468	LNCaP	prostate:	n/a
46	chr19:40169839-40169889	Hepatocyte	liver:	n/a
47	chr19:40168876-40168926	HCM	heart:	n/a
48	chr19:40169418-40169468	ovcar-3	ovarian:	n/a
49	chr19:40169839-40169889	SK-N-SH_RA	brain:	n/a
50	chr19:40174352-40174402	AoSMC	blood vessel:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40166471..40169299-chr19:40170755..40172585,2	K562	blood:
2	chr12:31226694..31227233-chr19:40172228..40172728,2	HCT-116	colon:
3	chr19:40172219..40174410-chr19:40181019..40183380,2	MCF-7	breast:
4	chr19:40168776..40170659-chr19:40171070..40173926,2	MCF-7	breast:
5	chr19:40166260..40168931-chr19:40253973..40255544,2	MCF-7	breast:
6	chr19:40168776..40170659-chr19:40171070..40173926,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGALS14-1	chr19:40175942-40176058	NR_034156
2	lnc-LGALS14-1	chr19:40175350-40175447	NR_034156
3	lnc-LGALS14-1	chr19:40174127-40174403	NR_034156
4	lnc-LGALS14-1	chr19:40176193-40176292	NR_034156
5	lnc-LGALS14-1	chr19:40175884-40176058	ENSG00000226025
6	lnc-LGALS14-1	chr19:40176825-40177013	NR_034156
7	lnc-LGALS14-1	chr19:40170014-40170074	NR_034156
8	lnc-LGALS14-1	chr19:40172073-40172149	NR_034156
9	lnc-LGALS14-1	chr19:40172638-40172848	NR_034156

No data

Variant related genes	Relation type
ENSG00000226025	TF binding region
ENSG00000269460	TF binding region
ENSG00000226025	CpG island
ENSG00000269460	CpG island
ENSG00000226025	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000013573	chromatin interactions

Extended variants
information (count: 412 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534190199	chr19:40168896-40168897	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs16973560	chr19:40168929-40168930	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs149843041	chr19:40168950-40168951	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs564106452	chr19:40168984-40168985	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs557231374	chr19:40168987-40168988	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs573025682	chr19:40168998-40168999	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs540285798	chr19:40169081-40169082	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77032450	chr19:40169082-40169083	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370981808	chr19:40169092-40169093	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs55976926	chr19:40169207-40169208	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs551148951	chr19:40169256-40169257	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs542924621	chr19:40169264-40169265	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs570923958	chr19:40169277-40169278	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs8113492	chr19:40169293-40169294	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs561606639	chr19:40169294-40169295	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs12463334	chr19:40169328-40169329	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs12985687	chr19:40169364-40169365	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs62119911	chr19:40169404-40169405	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs374609660	chr19:40169405-40169406	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533875891	chr19:40169418-40169419	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548761356	chr19:40169419-40169420	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs532607424	chr19:40169423-40169424	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs567352669	chr19:40169447-40169448	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs537673309	chr19:40169448-40169449	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs556308712	chr19:40169490-40169491	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs554886563	chr19:40169568-40169569	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368713654	chr19:40169577-40169578	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145878863	chr19:40169654-40169655	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs148969638	chr19:40169727-40169728	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs557735157	chr19:40169812-40169813	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs186549130	chr19:40169839-40169840	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191100314	chr19:40169840-40169841	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs62119912	chr19:40169845-40169846	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs142928760	chr19:40169908-40169909	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544510863	chr19:40169931-40169932	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563698233	chr19:40169954-40169955	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs146618822	chr19:40170009-40170010	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs8103033	chr19:40170053-40170054	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	mRNA abundance disease
39	rs556722644	chr19:40170079-40170080	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545668971	chr19:40170083-40170084	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs560199426	chr19:40170088-40170089	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11083532	chr19:40170103-40170104	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs548942905	chr19:40170106-40170107	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs572647850	chr19:40170137-40170138	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs79145143	chr19:40170139-40170140	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs141297334	chr19:40170150-40170151	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549731781	chr19:40170151-40170152	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571065820	chr19:40170213-40170214	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs548938929	chr19:40170219-40170220	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532717241	chr19:40170222-40170223	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40162600-40169600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:40166200-40169600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr19:40166200-40169600	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr19:40167400-40169600	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr19:40168000-40169800	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr19:40168200-40170000	Enhancers	Fetal Muscle Leg	muscle
7	chr19:40168200-40170400	Enhancers	Placenta	Placenta
8	chr19:40168400-40170200	Enhancers	Psoas Muscle	Psoas
9	chr19:40168400-40170600	Enhancers	Left Ventricle	heart
10	chr19:40168400-40170600	Enhancers	HepG2	liver
11	chr19:40168400-40171200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
12	chr19:40168600-40169200	Flanking Active TSS	Liver	Liver
13	chr19:40168600-40169200	Active TSS	Pancreatic Islets	Pancreatic Islet
14	chr19:40168600-40169400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr19:40168600-40169600	Enhancers	Duodenum Mucosa	Duodenum
16	chr19:40168600-40169800	Enhancers	Primary T cells fromperipheralblood	blood
17	chr19:40168600-40169800	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr19:40168600-40169800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr19:40168600-40170000	Enhancers	Gastric	stomach
20	chr19:40168600-40170400	Enhancers	Brain Anterior Caudate	brain
21	chr19:40168600-40170600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr19:40168600-40170600	Enhancers	Adipose Nuclei	Adipose
23	chr19:40168600-40170600	Enhancers	Lung	lung
24	chr19:40168600-40170600	Enhancers	Pancreas	Pancrea
25	chr19:40168600-40170600	Enhancers	Right Ventricle	heart
26	chr19:40168600-40170800	Enhancers	Rectal Mucosa Donor 29	rectum
27	chr19:40168600-40171600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr19:40168600-40172600	Flanking Active TSS	GM12878-XiMat	blood
29	chr19:40168800-40169000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr19:40168800-40169000	Enhancers	Colonic Mucosa	Colon
31	chr19:40168800-40169000	Flanking Active TSS	A549	lung
32	chr19:40168800-40169200	Weak transcription	Fetal Muscle Trunk	muscle
33	chr19:40168800-40169800	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr19:40168800-40169800	Weak transcription	Esophagus	oesophagus
35	chr19:40168800-40170800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
36	chr19:40168800-40171200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
37	chr19:40169000-40169800	Enhancers	Fetal Lung	lung
38	chr19:40169000-40169800	Enhancers	Small Intestine	intestine
39	chr19:40169000-40170200	Weak transcription	Colonic Mucosa	Colon
40	chr19:40169000-40170400	Enhancers	Colon Smooth Muscle	Colon
41	chr19:40169000-40171400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr19:40169200-40169400	Enhancers	Fetal Muscle Trunk	muscle
43	chr19:40169200-40169600	Enhancers	Liver	Liver
44	chr19:40169200-40169800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr19:40169200-40169800	Enhancers	Brain Substantia Nigra	brain
46	chr19:40169400-40169800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr19:40169400-40170000	Weak transcription	Fetal Muscle Trunk	muscle
48	chr19:40169400-40170400	Enhancers	Brain Hippocampus Middle	brain
49	chr19:40169400-40170400	Enhancers	Stomach Mucosa	stomach
50	chr19:40169600-40169800	Flanking Active TSS	Duodenum Mucosa	Duodenum

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